Skip to content

Brain-Behavior Interactions in Tic Suppression

Integrative Examination of Neurobehavioral Mechanisms in Tic Suppression

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02205918
Enrollment
30
Registered
2014-08-01
Start date
2017-07-01
Completion date
2019-09-01
Last updated
2020-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Motor Tic Disorder, Chronic Vocal Tic Disorder, Tourette's Syndrome

Brief summary

The purpose of this study is to examine how the brain and environment interact to influence children's ability to suppress tics using a medical technology called Transcranial Magnetic Stimulation (TMS).

Detailed description

Objectives: This study will recruit youth with chronic tics. Chronic tics are the most common movement disorder in children. The goal of the study is to learn how the brain and environment influence children's ability to suppress tics. Specifically, we want to learn how tics are influenced by a certain part of the brain called the supplementary motor area (SMA). This part of the brain is thought to be more active in people with tics. This will be the first study to look at the relationship between SMA, tic suppression, and urges to tic. Research Procedures: The study will take place over the course of three days within a week (about 5 hours total). The study will examine the relationship between the SMA and tic suppression using a non-invasive medical technology called Transcranial Magnetic Stimulation (TMS). Participants will have a diagnostic interview, MRI brain scan (used to find the location of the SMA), and TMS. Participants will be asked to try to suppress tics before and after TMS. The information that will be collected from participation includes information about tic symptoms, emotional and behavioral functioning, and brain activity (from MRI brain images and TMS results).

Interventions

There will be one, 30-minute TMS session. Participants randomly assigned to this group will receive 1hz active TMS. Tics and urges will be monitored immediately before and after TMS.

OTHERSham TMS

There will be one, 30-minute TMS session. Participants randomly assigned to this group will receive inactive (sham) TMS. Tics and urges will be monitored immediately before and after TMS.

Sponsors

University of Minnesota
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Presence of motor and/or vocal tics for at least one year * English fluency

Exclusion criteria

* Participants with medical conditions that are contraindicated for TMS (history of any known intracranial pathology, epilepsy or seizures, traumatic brain injury, brain tumor, stroke, implanted medical devices, current pregnancy or girls of childbearing age not using effective contraception, or any other serious medical conditions * Left-handedness * Previous diagnosis of psychosis, autism spectrum disorder, mental retardation, or cognitive disability * Inability to undergo MRI * Substance abuse or dependence within the past year * History of ≥3 sessions of Habit Reversal Therapy or other treatment primarily comprised of tic suppression strategies * Current suicidal intent * Current neuroleptic medications, as these medications are known to lower seizure threshold

Design outcomes

Primary

MeasureTime frameDescription
Tic frequencyDay 3Tics will be observed and counted

Secondary

MeasureTime frameDescription
Urge to ticDay 3The participant will be asked to give subjective ratings of premonitory urge intensity

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026